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| Product | Description | |
|---|---|---|
| Direct Red 80 | Direct Red 80. Group: Biochemicals. Grades: Highly Purified. CAS No. 2610-10-8. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. US Biological Life Sciences. |  Worldwide |
| Direct Red 80 | Direct Red 80 (Sirius Red) is a polyazo dye used principally in staining methods for collagen and amyloid. Direct Red 80 does not release benzidine upon degradation and is safer than many traditional direct dyes [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sirius Red. CAS No. 2610-10-8. Pack Sizes: 1 g. Product ID: HY-D0333. |  |
| Cetostearyl Alcohol | Cetostearyl alcohol occurs as white or cream-colored unctuous masses, flakes, pellets or granules. It has a faint, characteristic sweet odor. On heating, cetostearyl alcohol melts to a clear, colorless or pale yellow-colored liquid free of suspended matter. Synonyms: Alcohol cetylicus et stearylicus; cetearyl alcohol; cetyl stearyl alcohol; Crodacol CS90; Lanette O; Speziol C16-18 Pharma; Tego Alkanol 1618; Tego Alkanol 6855. CAS No. 8005-44-5. Product ID: PE-0531. Category: Emollient; Emulsifying Agents; Viscosity-increasing Agents. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0531; Cetostearyl Alcohol; Emollient; Emulsifying Agents; Viscosity-increasing Agents; ; 8005-44-5. UNII: 2DMT128M1S. Chemical Name: Cetostearyl alcohol. Grade: Pharmceutical Excipients. Administration route: Oral; topical; vaginal. Dosage Form: Oral tablets; topical emulsions, lotions, ointments; vaginal suppositories. Stability and Storage Conditions: Cetostearyl alcohol is stable under normal storage conditions. Cetostearyl alcohol should be stored in a well-closed container in a cool, dry place. Source and Preparation: Cetostearyl alcohol is prepared by the reduction of the appropriate fatty acids from vegetable and animal sources. Cetostearyl alcohol can also be prepared directly from hydrocarbon sources. Applications: Cetostearyl alcohol is used in cosmetics and topical pharmaceutical preparations. |  |
| mCAP | Used for in vitro transcription of 5'-capped mRNA to generate Cap 0 structure. mCAP has a 50% chance of inserting in the right direction to enhance translation. Another 50% of the molecules cannot become effective translation substrates, which reduces the specific activity of the transcript. Synonyms: m7G(5')ppp(5')G Cap Analog; N7-Methyl-Guanosine-5'-Triphosphate-5'-Guanosine; 7-Methyl-guanosine-5'-triphosphate-5'-guanosine; M7-GpppG. Grades: ≥90% by AX-HPLC. Molecular formula: C21H30N10O18P3 (free acid). Mole weight: 803.44 (free acid). |  |
| NADP-retinol dehydrogenase | Greater catalytic efficiency in the reductive direction. This observation, and the enzyme's localization at the entrance to the mitochondrial matrix, suggest that it may function to protect mitochondria against oxidative stress associated with the highly reactive retinal produced from dietary β-carotene by EC 1.13.11.63 (β-carotene 15,15'-dioxygenase). Km-values for NADP+ and NADPH are at least 800-fold lower than those for NAD+ and NADH. This enzyme differs from EC 1.1.1.105, retinol dehydrogenase, which prefers NAD+ and NADH. Group: Enzymes. Synonyms: all-trans retinal reductase (ambiguous); all-trans-retinol dehydrogenase; NADP(H)-dependent retinol dehydrogenase/reductase; RDH11; RDH12; RDH13; RDH14; retinol dehydrogenase 12; retinol dehydrogenase 14; retinol dehydrogenase [NADP+]; RalR1; PSDR1. Enzyme Commission Number: EC 1.1.1.300. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0211; NADP-retinol dehydrogenase; EC 1.1.1.300; all-trans retinal reductase (ambiguous); all-trans-retinol dehydrogenase; NADP(H)-dependent retinol dehydrogenase/reductase; RDH11; RDH12; RDH13; RDH14; retinol dehydrogenase 12; retinol dehydrogenase 14; retinol dehydrogenase [NADP+]; RalR1; PSDR1. Cat No: EXWM-0211. |  |
| REV-ERB Agonist II, SR9009 | A pyrrolidinecarbamate compound that acts as a specific REV-ERB-alpha/beta agonist. Exhibits a direct and reversible binding (Kd = 800nM REV-ERB-alpha) and shows excellent selectivity over a panel of 46 other nuclear receptors. Potently increases REV-ERB-dependent repressor activity (IC50 = 670 and 800nM in Gal4-REV-ERB-alpha and beta transfected HEK 293 cells) and reduces BMAL1 mRNA in HepG2 cells (IC50 = 710nM). Shown to cross the blood-brain barrier and exhibit desirable pharmacokinetic properties. A 7-day administration of SR9009 (100mg/kg, i.p., b.i.d.) causes a significant weight and fat loss in C57BL6 mice with concomitant reduction in plasma glucose and free fatty acid levels, and alters circadian pattern. 217739, CAS # 1379686-30-2, acts as a specific REV-ERB-α/ β agonist that exhibits a direct and reversible binding (Kd = 800nM). Group: Biochemicals. Grades: Highly Purified. CAS No. 1379686-30-2. Pack Sizes: 25mg. Molecular Formula: C??H??ClN?O?S. US Biological Life Sciences. | Worldwide |
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